Regulating the Topology of Covalent Organic Frameworks for Boosting Overall H2O2 Photogeneration

Photocatalytic oxygen reduction reactions and water oxidation reactions are extremely promising green approaches for massive H2O2 production. Nonetheless, constructing effective photocatalysts for H2O2 generation is critical and still challenging. Since the network topology has significant impacts on the electronic properties of two dimensional (2D) polymers, herein, for the first time, we regulated the H2O2 photosynthetic activity of 2D covalent organic frameworks (COFs) by topology. Through designing the linking sites of the monomers, we synthesized a pair of novel COFs with similar chemical components on the backbones but distinct topologies. Without sacrificial agents, TBD‐COF with cpt topology exhibited superior H2O2 photoproduction performance (6085 and 5448 μmol g−1 h−1 in O2 and air) than TBC‐COF with hcb topology through the O2‐O2⋅−‐H2O2, O2‐O2⋅−‐O21‐H2O2, and H2O‐H2O2 three paths. Further experimental and theoretical investigations confirmed that during the H2O2 photosynthetic process, the charge carrier separation efficiency, O2⋅− generation and conversion, and the energy barrier of the rate determination steps in the three channels, related to the formation of *OOH, *O21, and *OH, can be well tuned by the topology of COFs. The current study enlightens the fabrication of high‐performance photocatalysts for H2O2 production by topological structure modulation. By linking site design, two novel two dimensional covalent organic frameworks (COFs) with similar chemical constitutions but different topologies were constructed. TBD‐COF with six‐arm cores and cpt topology exhibited better H2O2 photosynthetic activity than TBC‐COF with three‐arm cores and hcb topology through the O2‐O2.−‐H2O2, O2‐O2.−‐O21‐H2O2, and H2O‐H2O2 three channels, inspiring regulating the topology of COFs for boosting overall H2O2 photogeneration.